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Title
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MIND : a double-linear model to accurately determine monoisotopic precursor mass in high-resolution top-down proteomics
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Author
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Abstract
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| Top-down proteomics approaches are becoming ever more popular, due to the advantages offered by knowledge of the intact protein mass in correctly identifying the various proteoforms that potentially arise due to point mutation, alternative splicing, post-translational modifications, etc. Usually, the average mass is used in this context; however, it is known that this can fluctuate significantly due to both natural and technical causes. Ideally, one would prefer to use the monoisotopic precursor mass, but this falls below the detection limit for all but the smallest proteins. Methods that predict the monoisotopic mass based on the average mass are potentially affected by imprecisions associated with the average mass. To address this issue, we have developed a framework based on simple, linear models that allows prediction of the monoisotopic mass based on the exact mass of the most-abundant (aggregated) isotope peak, which is a robust measure of mass, insensitive to the aforementioned natural and technical causes. This linear model was tested experimentally, as well as in silico, and typically predicts monoisotopic masses with an accuracy of only a few parts per million. A confidence measure is associated with the predicted monoisotopic mass to handle the off-by-one-Da prediction error. Furthermore, we introduce a correction function to extract the “true” (i.e., theoretically) most-abundant isotope peak from a spectrum, even if the observed isotope distribution is distorted by noise or poor ion statistics. |
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Language
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English
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Source (journal)
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Analytical chemistry. - Washington, D.C., 1948, currens
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Publication
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Washington, D.C.
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2019
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ISSN
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0003-2700
[print]
5206-882X
[online]
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DOI
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10.1021/ACS.ANALCHEM.9B02682
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Volume/pages
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91
:15
(2019)
, p. 10310-10319
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ISI
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000480499200131
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Pubmed ID
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31283196
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Full text (Publisher's DOI)
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Full text (open access)
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